Results 151 to 160 of about 4,029 (188)

Rosai-Dorfman Disease of the Lung

Respiratory Care, 2012
Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a benign proliferation of histiocytes. It was first described in 1969 by Rosai and Dorfman.[1][1] This disease mainly affects superficial and deep lymph nodes.
Hong, Ji, Bing, Zhang, Dong, Tian, Shuhua, Wu, Xia, Wang, Yuhong, Zhu   +5 more
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Rosai-Dorfman disease and uveitis

European Journal of Dermatology, 2017
Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare benign disease characterized by persistent massive lymphadenopathy caused by increased numbers of macrophages within lymph node sinuses [1, 2]. These cells are often large and exhibit abnormal behaviour, engulfing intact cells (such as lymphocytes ...
Natsuki, Nakajima, Takeshi, Fukumoto, Takeshi, Kozaru, Masanobu, Sakaguchi, Kazumi, Norose, Masahiro, Oka   +5 more
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Rosai-Dorfman Disease of the Breast

American Journal of Roentgenology, 2005
1All authors: Division of Diagnostic Imaging, University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Blvd., Box 57, Houston, TX 77030. Address correspondence to G. J. Whitman (gwhitman@di.mdacc.tmc.edu). 53-year-old woman presented with an ill-defined mass in the left breast on screening mammography.
Cynthia B, Pham, Lynne V, Abruzzo, Elise, Cook, Gary J, Whitman, Tanya W, Stephens   +4 more
openaire   +2 more sources

Rosai-Dorfman disease of the larynx

The Journal of Laryngology & Otology, 2000
We present a case of an 81-year-old man with a history of worsening dysphonia of six months duration. A year before a sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) was diagnosed on a submandibular lymph node biopsy. On presentation the patient showed a mass in the left subglottic area with a modest reduction in the airway ...
ALUFFI VALLETTI, Paolo, PIA, Francesco, Prestinari A, Ramponi A, Castri M   +4 more
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Intracranial Rosai–Dorfman disease

Journal of Clinical Neuroscience, 2016
Rosai-Dorfman disease (RDD) is a rare histioproliferative disorder that only occasionally involves the central nervous system. We present the diagnosis and treatment of five patients with intracranial RDD. The patients were preoperatively misdiagnosed as meningioma or eosinophilic granuloma.
Bo Yuan, Huang, Miao, Zong, Wen Jing, Zong, Yan Hui, Sun, Hua, Zhang, Hong Bo, Zhang   +5 more
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Rosai-Dorfman disease of the mandible

Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology, 2006
Rosai-Dorfman disease (RDD) is a rare, non-neoplastic histiocytosis most commonly characterized by painless, massive cervical lymphadenopathy. Over half of all patients with lymph node involvement also demonstrate extranodal disease, with most affected individuals exhibiting lesions within the region of the head and neck. Oral manifestations of RDD are
Faizan, Alawi, Brian T, Robinson, Lee, Carrasco   +2 more
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Cerebral Rosai–Dorfman disease

Child's Nervous System, 2015
Sinus histiocytosis (Rosai-Dorfman disease) with massive lymphadenopathy is a rare nonneoplastic and nonlangerhans cell proliferation disorder of the histiocytes. Extranodal location with or without lymphadenopathy occurs in about 40 % of the cases. Intracranial location is rare in children often mimicking meningiomas. The parasphenoidal region is more
Wolf, Lüdemann, Rouzbeh, Banan, Amir, Samii, Michalis, Koutzoglou, Concezio, Di Rocco   +4 more
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Rosai-Dorfman disease of the subglottis

The Journal of Laryngology & Otology, 2000
A case of subglottic narrowing caused by an extranodal deposit of sinus histiocytosis in a 29-year-old man is reported. The characteristic features of Rosai-Dorfman disease, such as massive painless cervical lymphadenopathy, fever, raised erythrocyte sedimentation rate and raised white cell count, were all found to be absent.
P, Hazarika, D R, Nayak, R, Balakrishnan, H G, Kundaje, P L, Rao   +4 more
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Rosai-Dorfman Disease

The Journal of the Association of Physicians of India, 2018
A young male presented with recurrent neck swellings with initial leucocyte count of 16800/mm3, with non-caseating glands on ultrasonography neck. FNAC showed mixed cellularity with histiocytic and marked lymphophagocytosis as seen in Rosai Dorfman Disease. Immunohistochemistry demonstrated CD 25, Ki 67 and CD 68 in histiocytes.
B N, Mahanta, T Goswami, Mahanta
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Castleman Disease and Rosai-Dorfman Disease

Seminars in Diagnostic Pathology, 2018
This chapter describes the main features of two different diseases, Castleman Disease (CD) and Rosai-Dorfman Disease (RDD). Castleman disease (CD) is a clinical and histopathologically heterogeneous lymphoproliferative disorder that encompasses at least three distinct entities with some common overlapping morphological features: Hyaline Vascular CD ...
Miguel A, Piris, Elena, Aguirregoicoa, Santiago, Montes-Moreno, Catuxa, Celeiro-Muñoz   +3 more
openaire   +2 more sources